Reglamentario: encuentra los mejores servicios

Reglamentario: obtén los mejores servicios freelance para completar tus proyectos con éxito.

7773 servicios disponibles

help pharmaceutical regulatory and bpom documents

A

I will help pharmaceutical regulatory and bpom documents

prepare regulatory affairs documents and medical articles

D

I will prepare regulatory affairs documents and medical articles

5.0(1)

write and optimize mhra and eu regulatory ectd documents

S

I will write and optimize mhra and eu regulatory ectd documents

provide regulatory labeling training for US eu smpc uspi ccds and tpl

T

I will provide regulatory labeling training for US eu smpc uspi ccds and tpl

do medical regulatory writing, ctd dossier, and fda ema compliance documentation

M

I will do medical regulatory writing, ctd dossier, and fda ema compliance documentation

do regulatory assignments related to ctd

M

I will do regulatory assignments related to ctd

5.0(1)

write fda 510k submission, clinical study report and regulatory documents

M

I will write fda 510k submission, clinical study report and regulatory documents

assess your financial services regulatory, risk or customer issue

L

Liz Larsson MBA

I will assess your financial services regulatory, risk or customer issue

write articles on regulatory affairs and pharmaceuticals

S

Nivel 1

I will write articles on regulatory affairs and pharmaceuticals

4.9(31)

do pharmacology, medicinal, regulatory, addiction and industrial

S

I will do pharmacology, medicinal, regulatory, addiction and industrial

provide regulatory affairs and compliance support

A

I will provide regulatory affairs and compliance support

J

I will design weekly regulatory blog logo

review and formate regulatory docs professionally

A

I will review and formate regulatory docs professionally

provide fda compliance and regulatory consulting

W

I will provide fda compliance and regulatory consulting

conduct legal regulatory research and compliance monitoring

M

I will conduct legal regulatory research and compliance monitoring

translate pharmaceutical, gmp, regulatory, and technical documents

Y

I will translate pharmaceutical, gmp, regulatory, and technical documents

prepare fda 510k submission and regulatory documents

E

I will prepare fda 510k submission and regulatory documents

provide regulatory compliance consulting for your business

D

I will provide regulatory compliance consulting for your business

write a professional regulatory affairs resume and cover letter

H

I will write a professional regulatory affairs resume and cover letter

write format clinical study report regulatory medical documents for cros pharma

M

I will write format clinical study report regulatory medical documents for cros pharma

provide fda regulatory compliance support for your product

I

I will provide fda regulatory compliance support for your product

support cmc, ectd and regulatory submissions globally

D

I will support cmc, ectd and regulatory submissions globally

assist in medical device regulatory submissions and certifications

L

I will assist in medical device regulatory submissions and certifications

5.0(3)

provide regulatory compliance and lab investigations

M

I will provide regulatory compliance and lab investigations

do perioperative nursing, assigned, regulatory affairs, renal nursing

N

I will do perioperative nursing, assigned, regulatory affairs, renal nursing

help in pharmaceuticals, nutraceutical, regulatory affairs, toxicology, illness

S

I will help in pharmaceuticals, nutraceutical, regulatory affairs, toxicology, illness

assist with US product compliance and regulatory documentation

G

I will assist with US product compliance and regulatory documentation

be your medical device regulatory and quality consultant

M

I will be your medical device regulatory and quality consultant

prepare ctd modules and cmc regulatory documents

M

I will prepare ctd modules and cmc regulatory documents

translate technical and regulatory documents english to japanese

S

I will translate technical and regulatory documents english to japanese

provide gdpr, compliance, and regulatory research for businesses

R

I will provide gdpr, compliance, and regulatory research for businesses

provide indonesia regulatory and bpom compliance consulting

A

I will provide indonesia regulatory and bpom compliance consulting

write medical, regulatory, and clinical research content

D

Dr. Haris Saeed

I will write medical, regulatory, and clinical research content

perform professional statutory research and regulatory compliance summaries

J

Jorge A. Gaitan

I will perform professional statutory research and regulatory compliance summaries

prepare healthcare fraud, stark law, and regulatory legal filings

C

I will prepare healthcare fraud, stark law, and regulatory legal filings

conduct regulatory compliance, compliance audit, notification, ingredient review

T

I will conduct regulatory compliance, compliance audit, notification, ingredient review

fda compliance, fda consulting, fda audit, quality compliance, regulatory, wcag

D

I will fda compliance, fda consulting, fda audit, quality compliance, regulatory, wcag

fixed ghl a2p or regulatory issue for your gohighlevel account

M

I will fixed ghl a2p or regulatory issue for your gohighlevel account

provide fda registration and regulatory compliance for medical devices

M

I will provide fda registration and regulatory compliance for medical devices

advise on italy, portugal company formation, eu regulatory

L

I will advise on italy, portugal company formation, eu regulatory

write expert clinical study reports and regulatory documents

D

I will write expert clinical study reports and regulatory documents

write professional articles on medical and regulatory affairs as a pharmacist

T

I will write professional articles on medical and regulatory affairs as a pharmacist

provide expert quality and regulatory consulting for medical devices

P

I will provide expert quality and regulatory consulting for medical devices

be your regulatory medical writer for fda and clinical dossiers

T

I will be your regulatory medical writer for fda and clinical dossiers

find and translate china legal documents and regulatory policies

J

I will find and translate china legal documents and regulatory policies

write professional articles on medical and regulatory affairs by a pharmacist

T

Nivel 1

I will write professional articles on medical and regulatory affairs by a pharmacist

4.9(6)

prepare healthcare fraud, stark law, and regulatory legal filings

L

Lawson Alphonse

I will prepare healthcare fraud, stark law, and regulatory legal filings

perform bsa, aml regulatory compliance audit

S

I will perform bsa, aml regulatory compliance audit

Desde USD 1,000

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